Total variants with conflicting interpretations: 7
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_002528. |
rs150766139 | 0.00138 |
NM_000152. |
rs142967546 | 0.00033 |
NM_000018. |
rs398123084 | 0.00014 |
NM_000492. |
rs747754623 | 0.00011 |
NM_170707. |
rs59301204 | 0.00004 |
NM_014946. |
rs878854991 | |
Single allele |